Cas 223552-13-4,dithiocarbonic acid <i>S</i>-{1-[3-(2,4-difluoro-phenyl)-3-oxo-propyl]-octyl} ester <i>O</i>-ethyl ester

223552-13-4

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Basic information

Product Name: dithiocarbonic acid S-{1-[3-(2,4-difluoro-phenyl)-3-oxo-propyl]-octyl} ester O-ethyl ester
Synonyms: dithiocarbonic acid S-{1-[3-(2,4-difluoro-phenyl)-3-oxo-propyl]-octyl} ester O-ethyl ester
CAS NO:223552-13-4
Molecular Formula:
Molecular Weight: 402.57
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: dithiocarbonic acid S-{1-[3-(2,4-difluoro-phenyl)-3-oxo-propyl]-octyl} ester O-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: dithiocarbonic acid S-{1-[3-(2,4-difluoro-phenyl)-3-oxo-propyl]-octyl} ester O-ethyl ester(223552-13-4)
EPA Substance Registry System: dithiocarbonic acid S-{1-[3-(2,4-difluoro-phenyl)-3-oxo-propyl]-octyl} ester O-ethyl ester(223552-13-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 223552-13-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 223552-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,5,5 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 223552-13:
(8*2)+(7*2)+(6*3)+(5*5)+(4*5)+(3*2)+(2*1)+(1*3)=104
104 % 10 = 4
So 223552-13-4 is a valid CAS Registry Number.

223552-13-4Upstream product

124-11-8 non-1-ene

223552-13-4Downstream Products

223552-13-4Relevant academic research and scientific papers

An unusual and highly efficient access to thieno[2,3-b]-benzothiopyran structures

Boivin, Jean,Boutillier, Peter,Zard, Samir Z.

, p. 2529 - 2532 (1999)

Dihydrothieno[2,3-b]-benzothiopyran-4-ones are easily obtained by an intermolecular radical addition to an unactivated olefin using an S-o- fluorophenacyl xanthate followed by a novel, base induced domino cyclisation.

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